638353-16-9 Usage
General Description
2,2-Bipyridine,6-methoxy-5-methyl-(9CI) is a chemical compound with the molecular formula C12H12N2O. It is a derivative of bipyridine, which is a heterocyclic organic compound. The 6-methoxy-5-methyl substitution on the bipyridine ring alters its chemical properties, making it useful in a variety of applications. 2,2-Bipyridine,6-methoxy-5-methyl-(9CI) may be used as a ligand in coordination chemistry, particularly in the formation of metal complexes. It has also been studied for its potential biological activity, including its role as an antioxidant and its ability to inhibit protein kinase activity. Additionally, 2,2-Bipyridine,6-methoxy-5-methyl-(9CI) has been investigated for its potential use in materials science, such as in the development of functionalized polymers or as a building block in organic synthesis. Overall, this compound has diverse potential applications in the fields of chemistry, biology, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 638353-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,8,3,5 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 638353-16:
(8*6)+(7*3)+(6*8)+(5*3)+(4*5)+(3*3)+(2*1)+(1*6)=169
169 % 10 = 9
So 638353-16-9 is a valid CAS Registry Number.
638353-16-9Relevant articles and documents
Reductive couplings of 2-halopyridines without external ligand: Phosphine-free nickel-catalyzed synthesis of symmetrical and unsymmetrical 2,2'-bipyridines
Liao, Lian-Yan,Kong, Xing-Rui,Duan, Xin-Fang
, p. 777 - 782 (2014/04/03)
An unexpectedly facile synthetic approach for symmetrical and unsymmetrical 2,2'-bipyridines through the Ni-catalyzed reductive couplings of 2-halopyridines was developed. The couplings were efficiently catalyzed by 5 mol % of NiCl2.6H2O without the use of external ligands. A variety of 2,2'-bipyridines including caerulomycin F have been efficiently synthesized.
Synthesis of Differently Disubstituted 2,2′-Bipyridines by a Modified Negishi Cross-Coupling Reaction
Luetzen, Arne,Hapke, Marko,Staats, Holger,Bunzen, Jens
, p. 3948 - 3957 (2007/10/03)
A general practical approach to a number of differently disubstituted 2,2′-bipyridines from substituted 2-bromo- and 2-chloropyridines by application of modified Negishi cross-coupling conditions has been developed. These 2,2′-bipyridines carry versatile functional groups that can be elaborated further, as demonstrated for some examples. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.
